Phenethyl bromide → HCID 67780719, compound
Reaction equation
[CH3:1][C:2]1[NH:10][C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[CH:3]=1.[Br:11][CH2:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C(#N)C>[BrH:11].[CH3:1][C:2]1[N:10]=[C:5]2[N:6]([CH2:12][CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH:7]=[CH:8][CH:9]=[C:4]2[CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 85 mg (0.64 mmol) of 2-methyl-pyrrolo[2,3-b]pyridine and 140 mg(0.76 mmol) of (2-bromoethyl)benzene in 1 ml acetonitrile was refluxed for 40 h. The solvent was evaporated and the residue was treated with ether. The solid that formed was isolated by filtration to give 188 mg (62%) of 2-methyl-7- (2-phenylethyl)pyrrolo[2,3-b]pyridinehydrobromide.
Workup
- customThe solvent was evaporated
- additionthe residue was treated with ether
- customThe solid that formed
- customwas isolated by filtration
Sources & evidence
- ORD record
- ord-f4a8dc231ed4479ab1db8ae1c538cb6f
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05439917
Reaction notes
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